5-Hydroxy-4-(p-hydroxybenzyl)-3'-3-dimethoxybibenzyl

Details

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Internal ID 74957122-9986-4b21-8021-1030d7f46ca1
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 2-[(4-hydroxyphenyl)methyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O4/c1-26-20-5-3-4-16(12-20)6-7-18-14-22(25)21(23(15-18)27-2)13-17-8-10-19(24)11-9-17/h3-5,8-12,14-15,24-25H,6-7,13H2,1-2H3
InChI Key AKPZBCLMSVLMLQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O4
Molecular Weight 364.40 g/mol
Exact Mass 364.16745924 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.49
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-4-(p-hydroxybenzyl)-3'-3-dimethoxybibenzyl

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9558 95.58%
Caco-2 + 0.5962 59.62%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.9257 92.57%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.8221 82.21%
OATP1B3 inhibitior + 0.9364 93.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8721 87.21%
P-glycoprotein inhibitior + 0.7314 73.14%
P-glycoprotein substrate + 0.6022 60.22%
CYP3A4 substrate + 0.5891 58.91%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.8279 82.79%
CYP2C9 inhibition + 0.5522 55.22%
CYP2C19 inhibition + 0.8362 83.62%
CYP2D6 inhibition - 0.7974 79.74%
CYP1A2 inhibition + 0.8281 82.81%
CYP2C8 inhibition + 0.9360 93.60%
CYP inhibitory promiscuity + 0.7644 76.44%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6654 66.54%
Carcinogenicity (trinary) Non-required 0.6737 67.37%
Eye corrosion - 0.9679 96.79%
Eye irritation - 0.4818 48.18%
Skin irritation - 0.7751 77.51%
Skin corrosion - 0.8656 86.56%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7861 78.61%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8425 84.25%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6581 65.81%
Acute Oral Toxicity (c) III 0.7335 73.35%
Estrogen receptor binding + 0.8889 88.89%
Androgen receptor binding + 0.8823 88.23%
Thyroid receptor binding + 0.7044 70.44%
Glucocorticoid receptor binding + 0.8728 87.28%
Aromatase binding - 0.5165 51.65%
PPAR gamma + 0.7816 78.16%
Honey bee toxicity - 0.7425 74.25%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9517 95.17%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 97.81% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.44% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 95.79% 95.17%
CHEMBL2535 P11166 Glucose transporter 94.22% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.45% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.44% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.10% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.78% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.73% 86.33%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.51% 96.09%
CHEMBL240 Q12809 HERG 90.81% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.74% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.66% 94.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 88.97% 99.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.55% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.45% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.16% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 86.82% 90.20%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.78% 86.92%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.70% 96.95%
CHEMBL4208 P20618 Proteasome component C5 86.13% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 83.25% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.76% 94.45%
CHEMBL1921 P47901 Vasopressin V1b receptor 82.08% 92.50%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.08% 92.67%
CHEMBL4101 P17612 cAMP-dependent protein kinase alpha-catalytic subunit 80.59% 82.86%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Syzygium aromaticum

Cross-Links

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PubChem 5318227
NPASS NPC120247